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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Part 607 — ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
Subpart C — Procedures for Foreign Blood Product Establishments
Federal (United States) · Regulations
Subpart C — Procedures for Foreign Blood Product Establishments
1 section
1 section
21 C.F.R. § 607.40
Establishment registration and blood product listing requirements for foreign blood product establishments.
Subpart C — Procedures for Foreign Blood Product Establishments | Federal (United States) Regulations | Justis AI